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Drucker Labs LP

1 recall record in Other.

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2012

1 record

Class IITerminatedRecall F-2126-2012

Product description

intraKID Lot 658 with a Best By date of 12/12, 33 oz and 2 oz bottles

Reason for recall

After extensive testing and investigation, Drucker Labs has determined that an incorrect form of Vitamin B3, Nicotinic Acid, was used in the manufacturing of intraKID Lot 658. This nutrient may cause a temporary symptom in a small number of consumers. This symptom, commonly known as Niacin Flush, may include itching, redness, or warmth of the skin. This typically subsides within 15  20 minut

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Event ID
62872
Code info
Lot 658 with a Best By date of 12/12
Product quantity
2026 bottles
Distribution pattern
Nationwide and to Canada
Voluntary / mandated
Voluntary: Firm initiated
Initial firm notification
Letter
Product type
Food
Recalling firm location
1600 Capital Ave Ste 100, N/A, Plano, TX, United States
Recall initiation date
08/13/2012
Center classification date
09/05/2012
Termination date
10/07/2014